Canonical Allele Identifier: CA10376252
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs755657305
gnomAD v2: X-30322682-T-C
gnomAD v3: X-30304565-T-C
gnomAD v4: X-30304565-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304565T>C , CM000685.2:g.30304565T>C GRCh38
NC_000023.10:g.30322682T>C , CM000685.1:g.30322682T>C GRCh37
NC_000023.9:g.30232603T>C NCBI36
NG_009814.1:g.9814A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*14A>G MANE Select ENSP00000368253.4:n.*14A>G
ENST00000378970.4:c.*14A>G ENSP00000368253.4:n.*14A>G
NM_000475.4:c.*14A>G NP_000466.2:n.*14A>G
NM_000475.5:c.*14A>G MANE Select NP_000466.2:n.*14A>G